Rapidly Progressive Thalamic Dementia
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Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004
Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
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Niemann-Pick Disease Type C
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023
The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022
Adult-Onset Niemann-Pick Disease Type C Masquerading As Spinocerebellar Ataxias
Mol Genet Genomic Med 10:e1906, Vo,M.L.,et al, 2022
A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019
Neurodegeneration with Brain Iron Accumulation
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019
Atypical Presentations of Intracranial Hypotension: Comparison with Classic Spontaneous Intracranial Hypotension
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Wilson Disease
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015
Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015
Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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A 23-Year-Old Man With Seizures and Visual Deficit
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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Neurologic Manifestations in Welders with Pallidal MRI T1 Hyperintensity
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Clinicopath Conf, Multiple-System Atrophy
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Niemann-Pick Disease Type C: Two Cases and an Update
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Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
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Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
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Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
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GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
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Delayed Encephalopathy after Acute Carbon Monoxide Intoxication:MR Imaging Features & Cerebral White Matter Lesions
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Cortical Lewy Body Dementia:Clinical Features and Classification
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Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989
Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989
Diffuse Lewy Body Disease and Progressive Dementia
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Neurologic Aspects of Boxing
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Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
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Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
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Chediak-Higashi Syndrome
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Nervous System Toxicity of Chemo Agents
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Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
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Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
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A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
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Neurologic Manifestations of Hyperthyroidism and Graves Disease
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Risk of Parkinson Disease Among Service Members at Marine Corps Base Camp Lejeune
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Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
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A Middle-Aged Man with Progressive Gait Abnormalities
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